A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844978



Internal ID22619913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:47020282..47024019hg38UCSC Ensembl
chr6:46988018..46991755hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg383738
hg193738
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505854
Samples
Known GenesGPR110
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844978
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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